chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 140839133 140839134 G T 29 GENIC homozygous 112858094 4 140844030 140844031 A G 32 GENIC homozygous 112858098 4 140848282 140848283 T C 16 GENIC homozygous 113057483 4 140850025 140850026 G A 40 GENIC homozygous 113057485 4 140850323 140850324 C T 31 GENIC homozygous 113057487 4 140850486 140850487 T G 31 GENIC homozygous 112858108 4 140853035 140853036 T G 51 GENIC homozygous 113057495 4 140855052 140855053 T C 26 GENIC homozygous 112858124 4 140855327 140855328 T C 13 GENIC homozygous 112858128 4 140856740 140856741 T C 32 GENIC homozygous 112858140 4 140856804 140856805 C T 31 GENIC homozygous 113057499 4 140856874 140856875 C T 35 GENIC homozygous 113057501 4 140857084 140857085 G A 39 GENIC homozygous 113057503 4 140857526 140857527 C T 28 GENIC homozygous 113057507 4 140858330 140858331 C G 22 GENIC homozygous 112858148 4 140859256 140859257 G C 21 GENIC homozygous 112858152 4 140862482 140862483 G T 19 GENIC homozygous 112858154 4 140862554 140862555 A T 18 GENIC homozygous 113057509 4 140862644 140862645 A G 17 GENIC homozygous 113057511 4 140865458 140865459 A G 28 GENIC homozygous 112858156 4 140866714 140866715 A G 23 GENIC homozygous 113057513 4 140873341 140873342 A T 39 GENIC homozygous 112858162 4 140876205 140876206 G A 29 GENIC homozygous 112858164 4 140876462 140876463 C G 26 GENIC homozygous 112858166